Pharmaceutical manufacturing experience is highly preferred, especially equipment used in injectable/filling-line operations . 1–2 years of experience, ideally around 1.5 years , in Life Sciences, Pharmaceutical Manufacturing, or a related regulated environment.
Numbers & Facts
Location
Chicago, Illinois
Description
Technical Writer – Validation
Location: Melrose Park, IL | 100% Onsite Type: 6-Month Contract-to-Hire Start: ASAP
Ideal Candidate:
1–2 years of experience, ideally around 1.5 years, in Life Sciences, Pharmaceutical Manufacturing, or a related regulated environment.
Experience creating, reviewing, or maintaining technical/validation documentation.
Exposure to equipment validation, process validation, IQ/OQ/PQ, protocols, reports, SOPs, and GMP documentation.
Pharmaceutical manufacturing experience is highly preferred, especially equipment used in injectable/filling-line operations.
Familiarity with MES systems, particularly PAS-X, is a strong plus.
Candidates with strong college accomplishments, internships, projects, or early-career achievements should be considered.
Excellent writing, documentation, organization, communication, and attention to detail.
Determination, attitude, adaptability, and willingness to learn will be critical.
Must be comfortable working 100% onsite in Melrose Park, Illinois.